A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3496e59



Internal ID22764716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40349835..40351233hg38UCSC Ensembl
chr6:40317574..40318972hg19UCSC Ensembl
chr6:40425552..40426950hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3399718, esv3354039, esv3354056
SamplesNA19238, NA19239, NA19240
Known GenesLINC00951
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3496e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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